Simplified gyral pattern

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Simplified gyral pattern (in one patient) [OMIM:Simplified gyral pattern (in one patient)]
Quality:
Cross references:
OMIM: "Simplified gyral pattern" [OMIM:Simplified gyral pattern]
OMIM: "Simplified gyral pattern (in one patient)" [OMIM:Simplified gyral pattern (in one patient)]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

ASPARAGINE SYNTHETASE DEFICIENCY (OMIM:615574)
CEREBROOCULOFACIOSKELETAL SYNDROME 4 (OMIM:610758)
MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS (OMIM:604317)
MICROCEPHALY 3, PRIMARY, AUTOSOMAL RECESSIVE (OMIM:604804)
MICROCEPHALY 9, PRIMARY, AUTOSOMAL RECESSIVE (OMIM:614852)
Microcephaly - seizures - developmental delay (Orphanet:228418)
Microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome (Orphanet:329332)
Microlissencephaly (Orphanet:1083)
Primary microcephaly-epilepsy-permanent neonatal diabetes syndrome (Orphanet:306558)
RETT SYNDROME, CONGENITAL VARIANT (OMIM:613454)
VAN MALDERGEM SYNDROME 1 (OMIM:601390)